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肠道微生态介导代谢相关脂肪性肝病演进的机制与肝病肠治策略
作者: style="font-size: 12px ">雷诗颖 郑晓皎 
单位:上海交通大学医学院附属第六人民医院 转化医学中心 上海 200233 
关键词:肠道微生态 代谢相关脂肪性肝病 肠-肝轴 
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出版年,卷(期):页码:2026,18(2):9-17
摘要:

 摘要:代谢相关脂肪性肝病(metabolic associated fatty liver disease,MAFLD)是全球最常见的慢性肝病,可进展为脂肪性肝炎、肝硬化及肝细胞癌。最近研究表明肠-肝轴失调是驱动 MAFLD 的上游因素之一。在 MAFLD 进展过程中,肠道微生物组呈现特征性改变,微生物及其结构、微生物源性外膜囊泡、酶和代谢物通过受损的肠道屏障驱动 MAFLD 发展。靶向肠-肝轴的策略(补充肠道微生物、益生元、后生元、胆汁酸等微生物代谢物)可通过改善肠道屏障和代谢缓解 MAFLD。未来需基于患者肠道微生物特征进行分层,深入开展多中心纵向研究,推动肠-肝轴靶向治疗在 MAFLD 精准医疗中的应用。

 Abstract: Metabolic associated fatty liver disease (MAFLD) is the most common chronic 

liver disease worldwide and can progress to steatohepatitis, cirrhosis and hepatocellular 
carcinoma. Recent studies showed that gut-liver axis dysregulation was one of the upstream 
factors driving MAFLD. During MAFLD progression, the intestinal microbiome exhibited 
characteristic alterations, and microorganisms along with their structures, microbe-derived 
outer membrane vesicles, enzymes and metabolites drive MAFLD development through a 
compromised intestinal barrier. Strategies targeting the gut-liver axis, such as supplementation 
with intestinal microbes, prebiotics, postbiotics, bile acids and other microbial metabolites, 
alleviated MAFLD by improving intestinal barrier integrity and metabolism. Future ef forts 
should stratify patients based on their gut microbiome characteristics, conduct in-depth 
multicenter longitudinal studies, and advance the application of gut-liver axis-targeted 
therapies in precision medicine for MAFLD.
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